DISCRENE SELF-SUPPORTING BREAST FORM
K-Number: K904086 · 1990-10-02
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Device Summary
Frequently Asked Questions
What is the DISCRENE SELF-SUPPORTING BREAST FORM?
DISCRENE SELF-SUPPORTING BREAST FORM is a medical device that received FDA 510(k) clearance on 1990-10-02. The listed applicant is Coloplast A/S. The 510(k) number is K904086.
When did DISCRENE SELF-SUPPORTING BREAST FORM receive FDA 510(k) clearance?
DISCRENE SELF-SUPPORTING BREAST FORM received FDA 510(k) clearance on 1990-10-02, under 510(k) number K904086.
Who is the listed applicant for DISCRENE SELF-SUPPORTING BREAST FORM?
The FDA 510(k) record lists Coloplast A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISCRENE SELF-SUPPORTING BREAST FORM?
The FDA product code for DISCRENE SELF-SUPPORTING BREAST FORM is KCZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Coloplast A/S as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KCZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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